檢驗和試驗控制程序-資料下載頁
2025-08-23 05:41本頁面
【正文】 行《質(zhì)量記錄控制程序》。All sampling, inspection, test and report should be pleted within the specified time limit. The record should be kept factually in standard form, and be kept by a special person. Implement the “Quality Record Control Procedures”. 檢驗和試驗全過程發(fā)現(xiàn)的不合格，執(zhí)行《不合格品控制程序》。Implement “Nonconforming Product Control Procedures” in case any nonconformance is found in the whole process of inspection and test. 檢驗和試驗過程中，要作好各類狀態(tài)標識，執(zhí)行《檢驗和試驗狀態(tài)控制程序》。In inspection and test process, make all necessary status labels properly and implement “Inspection amp。 Test Status Control Procedures”. 所有檢驗人員都要求經(jīng)過培訓合格后持證上崗。All the inspectors should be trained and certified for the post.5 相關文件Specific Document AICQ/WI100101 《檢驗要求》 AICQ/WI100101 “Inspection Requirements” AICQ/WI100102 《通用檢驗規(guī)程》 AICQ/WI100102 “General Inspection Regulation” AICQ/QP1301 《不合格品控制程序》 AICQ/QP1301 “Unacceptable Parts Control Procedure” AICQ/QP1201 《檢驗和試驗狀態(tài)控制程序》 AICQ/QP1201 “Inspection and Test Status Control Procedure” AICQ/WI1601 《 質(zhì)量記錄控制程序》 AICQ/WI1601 “Quality Record Control Procedure”6 質(zhì)量記錄Quality Records AICQ/QR100101A 《檢驗記錄表》 AICQ/QR100101A “Inspection Record Sheet” AICQ/QR100102A 《緊急例外放行申請單》 AICQ/QR100102A “Emergency Release Application Form” AICQ/QR100105A 《產(chǎn)品最終審核記錄表》AICQ/QR100105A Record Sheet of Product Final Audit AICQ/QR100107A 《產(chǎn)品合格通知單》 AICQ/QR100107A “Acceptable Parts Notice”更多資料下載 請到學習人家
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